Terms: = Germ cell tumor AND WRN, RECQL2, 7486, ENSG00000165392, Q14191, RECQ3
23 results:
1. Presumed Pathogenic germ Line and Somatic Variants in African American Thyroid Cancer.
Hurst ZA; Liyanarachchi S; Brock P; He H; Nabhan F; Veloski C; Toland AE; Ringel MD; Jhiang SM
Thyroid; 2024 Mar; 34(3):378-387. PubMed ID: 38062767
[No Abstract] [Full Text] [Related]
2. Flap endonuclease 1 and DNA-PKcs synergistically participate in stabilizing replication fork to encounter replication stress in glioma cells.
Zhang J; Chen M; Pang Y; Cheng M; Huang B; Xu S; Liu M; Lian H; Zhong C
J Exp Clin Cancer Res; 2022 Apr; 41(1):140. PubMed ID: 35414100
[TBL] [Abstract] [Full Text] [Related]
3. Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families.
Fidalgo F; Torrezan GT; Sá BCS; Barros BDF; Moredo LF; Valieris R; de Souza SJ; Duprat JP; Krepischi ACV; Carraro DM
PLoS One; 2022; 17(1):e0262419. PubMed ID: 35085295
[TBL] [Abstract] [Full Text] [Related]
4. Construction of a SUMOylation regulator-based prognostic model in low-grade glioma.
Li X; Meng Y
J Cell Mol Med; 2021 Jun; 25(12):5434-5442. PubMed ID: 33951297
[TBL] [Abstract] [Full Text] [Related]
5. Pharmacological targeting of differential DNA repair, radio-sensitizes wrn-deficient cancer cells in vitro and in vivo.
Gupta P; Saha B; Chattopadhyay S; Patro BS
Biochem Pharmacol; 2021 Apr; 186():114450. PubMed ID: 33571504
[TBL] [Abstract] [Full Text] [Related]
6. Inherited Follicular Epithelial-Derived Thyroid Carcinomas: From Molecular Biology to Histological Correlates.
Cameselle-Teijeiro JM; Mete O; Asa SL; LiVolsi V
Endocr Pathol; 2021 Mar; 32(1):77-101. PubMed ID: 33495912
[TBL] [Abstract] [Full Text] [Related]
7. Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance.
Fransson S; Martinez-Monleon A; Johansson M; Sjöberg RM; Björklund C; Ljungman G; Ek T; Kogner P; Martinsson T
Sci Rep; 2020 Dec; 10(1):22432. PubMed ID: 33384420
[TBL] [Abstract] [Full Text] [Related]
8. A deep analysis using panel-based next-generation sequencing in an Ecuadorian pediatric patient with anaplastic astrocytoma: a case report.
García-Cárdenas JM; Zambrano AK; Guevara-Ramírez P; Guerrero S; Runruil G; López-Cortés A; Torres-Yaguana JP; Armendáriz-Castillo I; Pérez-Villa A; Yumiceba V; Leone PE; Paz-Y-Miño C
J Med Case Rep; 2020 Aug; 14(1):136. PubMed ID: 32867815
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9. Prostatic carcinoma with neuroendocrine differentiation harboring the EWSR1-FEV fusion transcript in a man with the wrn G327X germline mutation: A new variant of prostatic carcinoma or a member of the Ewing sarcoma family of tumors?
Febres-Aldana CA; Krishnamurthy K; Delgado R; Kochiyil J; Poppiti R; Medina AM
Pathol Res Pract; 2020 Feb; 216(2):152758. PubMed ID: 31831298
[TBL] [Abstract] [Full Text] [Related]
10. Multimodal brain tumor image segmentation using wrn-PPNet.
Wang Y; Li C; Zhu T; Zhang J
Comput Med Imaging Graph; 2019 Jul; 75():56-65. PubMed ID: 31154088
[TBL] [Abstract] [Full Text] [Related]
11. Genes, Proteins, and Biological Pathways Preventing Chromothripsis.
Poot M
Methods Mol Biol; 2018; 1769():231-251. PubMed ID: 29564828
[TBL] [Abstract] [Full Text] [Related]
12. [Hereditary thyroid carcinoma and its molecular diagnostics].
Dvořáková S; Václavíková E; Sýkorová V; Hálková T; Bendlová B
Cesk Patol; 2014 Apr; 50(2):81-6. PubMed ID: 24758503
[TBL] [Abstract] [Full Text] [Related]
13. [Application of novel clinicopathological biomarkers].
Chano T
Rinsho Byori; 2012 Feb; 60(2):167-73. PubMed ID: 22568098
[TBL] [Abstract] [Full Text] [Related]
14. [Hereditary bone tumors].
Jundt G; Baumhoer D
Pathologe; 2010 Oct; 31(6):471-6. PubMed ID: 20960198
[TBL] [Abstract] [Full Text] [Related]
15. Identification of modifier genes for cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations.
Yang XR; Pfeiffer RM; Wheeler W; Yeager M; Chanock S; Tucker MA; Goldstein AM
Int J Cancer; 2009 Dec; 125(12):2912-7. PubMed ID: 19626699
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16. wrn Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brazil.
Pinto GR; Yoshioka FK; Clara CA; Santos MJ; Almeida JR; Burbano RR; Rey JA; Casartelli C
J Neurooncol; 2008 Dec; 90(3):253-8. PubMed ID: 18670736
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17. A case of Werner syndrome with three primary lesions of malignant melanoma.
Shibuya H; Kato A; Kai N; Fujiwara S; Goto M
J Dermatol; 2005 Sep; 32(9):737-44. PubMed ID: 16361718
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18. The Werner syndrome protein confers resistance to the DNA lesions N3-methyladenine and O6-methylguanine: implications for wrn function.
Blank A; Bobola MS; Gold B; Varadarajan S; D Kolstoe D; Meade EH; Rabinovitch PS; Loeb LA; Silber JR
DNA Repair (Amst); 2004 Jun; 3(6):629-38. PubMed ID: 15135730
[TBL] [Abstract] [Full Text] [Related]
19. Regulators of G-protein signaling 3 and 4 (RGS3, RGS4) are associated with glioma cell motility.
Tatenhorst L; Senner V; Püttmann S; Paulus W
J Neuropathol Exp Neurol; 2004 Mar; 63(3):210-22. PubMed ID: 15055445
[TBL] [Abstract] [Full Text] [Related]
20. Antagonism of buthionine sulfoximine cytotoxicity for human neuroblastoma cell lines by hypoxia is reversed by the bioreductive agent tirapazamine.
Yang B; Keshelava N; Anderson CP; Reynolds CP
Cancer Res; 2003 Apr; 63(7):1520-6. PubMed ID: 12670899
[TBL] [Abstract] [Full Text] [Related]
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